| Literature DB >> 21481773 |
Tzu-Lan Yeh1, Chih-Yung S Lee, L Mario Amzel, Peter J Espenshade, Mario A Bianchet.
Abstract
Fission yeast protein Sre1, the homolog of the mammalian sterol regulatory element-binding protein (SREBP), is a hypoxic transcription factor required for sterol homeostasis and low-oxygen growth. Nro1 regulates the stability of the N-terminal transcription factor domain of Sre1 (Sre1N) by inhibiting the action of the prolyl 4-hydroxylase-like Ofd1 in an oxygen-dependent manner. The crystal structure of Nro1 determined at 2.2 Å resolution shows an all-α-helical fold that can be divided into two domains: a small N-terminal domain, and a larger C-terminal HEAT-repeat domain. Follow-up studies showed that Nro1 defines a new class of nuclear import adaptor that functions both in Ofd1 nuclear localization and in the oxygen-dependent inhibition of Ofd1 to control the hypoxic response.Entities:
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Year: 2011 PMID: 21481773 PMCID: PMC3086001 DOI: 10.1016/j.str.2011.01.017
Source DB: PubMed Journal: Structure ISSN: 0969-2126 Impact factor: 5.006